Infrared to visible upconversion luminescence in Er3+/Yb3+ doped titanate glass prepared by containerless processing

Er³⁺ doped TiO₂–La₂O₃ glasses modified by ZrO₂ have been successfully fabricated by the containerless method with incorporated Yb³⁺ ions as sensitizers. Under the excitation of 980 and 808 nm diode lasers, visible emissions centered at 534, 554 and 674 nm are observed, which are assigned to the Er³⁺ transitions of ²H_11/2→⁴I_15/2, ⁴S_3/2→⁴I_15/2 and ⁴F_9/2→⁴I_15/2, respectively. The emission signals are so strong that they can be observed by naked eyes even at pumping power as low as 20 mW. Measurements of pump-power dependent intensity and time-resolved decay behavior of upconversion luminescence show that two-photon excited state absorption (ESA) and energy transfer (ET) between rare earth ions are the predominant mechanisms for upconversion emissions. Besides, the intensity of upconversion luminescence has been enhanced by increasing the concentration of ZrO₂ in these rare earth doped bulk titanate glasses.     

A space-dependent atomic superfluid current in Bose–Einstein condensates

A space-dependent atomic superfluid current with an explicit analytical expression and its role in Bose–Einstein condensates are studied. The factors determining the intensity and oscillating amplitude of the space-dependent atomic superfluid current are explored in detail. Research findings reveal that the intensity of the current can be regulated by setting an appropriate configuration of the trap and its oscillating amplitude can be adjusted via Feshbach resonance. It is numerically demonstrated that the space-dependent atomic superfluid current can exert great influence on the spatial distribution of condensed atoms, and even force condensed atoms into very complex distributional states with spatial chaos.     

微光夜视技术的现状和发展设想

评述微光夜视技术的现状和发展趋势，重点根据国外微光夜视技术发展水平，提出了我国发展此项技术的几点建议。     

模拟电子技术教学改革探讨

模拟电子技术是工科类学生的一门专业基础课程,与实践联系紧密,由于课程本身物理概念抽象,学习起来比较枯燥,使得学生普遍反映该门课程入门难、学习难.鉴于此本文在介绍如何提高课堂教学质量的同时着重提出小课题实验教学,通过简单的实验项目,帮助学生从直观上认识半导体器件,将各知识点串联起来,引导学生入门,激发学生学习兴趣.     

Structural,electronic, and optical properties of phenol‐pyridyl boron complexes for light‐emitting diodes

The coordination chemistry of polydentate chelating ligands that contain mixed pyridinephenol donor sets has been a sought‐after target of study and is a possible extension to the chemistry of polypyridines. In this article, seven compounds, which are the four‐coordinate boron complexes containing the mixed phenol‐pyridyl group, have been studied by theoretical calculation. They can function as charge transport materials and emitters, with high efficiency and stability. To reveal the relationship between the structures and properties of these bifunctional or multifunctional electroluminescent materials, the ground and excited state geometries were optimized at the B3LYP/6‐31G(d), HF/6‐31G(d), and CIS/6‐31G(d) levels, respectively. The ionization potentials (IPs) and electron affinities (EAs) were computed. The mobilities of hole and electron in these compounds were studied computationally based on the Marcus electron transfer theory. The lowest excitation energies, and the maximum absorption and emission wavelengths of these compounds were calculated by time‐dependent density functional theory method. As a result of these calculations, the values of HOMO, LUMO, energy gaps, IPs, EAs, and the balance between the hole‐ and electron‐transfer are greatly improved with the substitution of carbazole in compound 6 . The calculated emission spectra of the seven studied molecules can almost cover the full UV‐vis range (from 447.4 to 649.3 nm). Also, the Stokes shifts are unexpectedly large, ranging from 139.4 to 335.1 nm. This will result in the relatively long fluorescence lifetimes. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2009     

基于PAMAM/聚2,6-吡啶二甲酸膜DNA电化学生物传感器的制备及对禽病毒基因检测的研究

以铂电极上聚合的2,6-吡啶二甲酸(PDC)膜组装G5.0树状高分子(PAMAM)固定ssDNA探针, 制备了一种新型的DNA电化学生物传感器. 用[Fe(CN)6]3－/4－作氧化还原指示剂, 以电化学交流阻抗和循环伏安技术对探针ssDNA的固定和杂交进行了表征. 实验表明, 当ssDNA在复合膜上固定及与其互补序列杂交后, 电极表面的传递电阻(Ret)依次增大. 因此, 可以利用Ret的明显差异, 以此固定探针的修饰电极, 对互补序列DNA进行无标记交流阻抗检测. 基于该生物传感器结合交流阻抗技术对禽病毒基因进行检测, 在优化实验条件下, 靶基因ssDNA-2在2.0×10－11～1.0×10－8 mol•L－1线性范围内, 其浓度与电极表面的电子传递电阻(Ret)之间呈良好的线性关系, 检测限为3.6×10－12 mol•L－1. 表明该方法为病毒灵敏地检测提供了一个有益的传感平台.     

Bounded Tiles in ℚp are Compact Open Sets

Any bounded tile of the field Qp of p-adic numbers is a compact open set up to a set of zero Haar measure.In this note,we present two simple and direct proofs of this fact.     

Comments on ‘An efficient iterative method for solving the matrix equation AXB+CYD=E’

In this note, a technical error is pointed out in the proof of a lemma in the above paper. A correct proof of this lemma is given. In addition, a further result on the algorithm in the above paper is also given. Copyright © 2009 John Wiley & Sons, Ltd.     

Synergistic Doping and Intercalation: Realizing Deep Phase Modulation on MoS2 Arrays for High‐Efficiency Hydrogen Evolution Reaction

A synergistic N doping plus PO₄^3? intercalation strategy is used to induce high conversion (ca. 41 %) of 2H‐MoS₂ into 1T‐MoS₂, which is much higher than single N doping (ca. 28 %) or single PO₄^3? intercalation (ca. 10 %). A scattering mechanism is proposed to illustrate the synergistic phase transformation from the 2H to the 1T phase, which was confirmed by synchrotron radiation and spherical aberration TEM. To further enhance reaction kinetics, the designed (N,PO₄^3?)‐MoS₂ nanosheets are combined with conductive vertical graphene (VG) skeleton forming binder‐free arrays for high‐efficiency hydrogen evolution reaction (HER). Owing to the decreased band gap, lower d‐band center, and smaller hydrogen adsorption/desorption energy, the designed (N,PO₄^3?)‐MoS₂/VG electrode shows excellent HER performance with a lower Tafel slope and overpotential than N‐MoS₂/VG, PO₄^3?‐MoS₂/VG counterparts, and other Mo‐base catalysts in the literature.